Study Coordinator

Roles

• Prepare study documents for Ethics committee review and approval;
• Schedule the on-site visits with the Sponsor;
• Performing study socialization and planning subject recruitment strategy;
• Coordinating subjects recruitment and screening;
• Schedule subject visit and coordinating study activities with field team, laboratory, nutritionist, and all related study personnel;
• Oversee the storage and accountability of Investigational Product;
• Maintain accurate and complete records;
• Close the study and archive the study records;

Requirements

• Physician or other related medical background;
• Fluent in English are preferred;
• Have a good understanding and knowledge of Good Clinical Practice (GCP) and experiences in clinical trials are preferred;
• Able to organize a team or a group of trials participants;
• Have a good communication skill and interpersonal skill;
• Able to solve problems;
• Responsive, creative, and adaptable to manage changes;
• Fresh graduate are welcome to apply;

Please send your CV and Application Letter by email with subject: “Study Coordinator” (space) “Applicant Name “